FDA UDI In Commercial Distribution 🇺🇸 United States

Trilor

DI: 08056099232152 · Model: FDZ20PP · BIOLOREN SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trilor
Primary DI
08056099232152
Version / Model
FDZ20PP
Company Name
BIOLOREN SRL
Labeler DUNS
428561679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-13
Public Version
1
Public Version Date
2021-09-21
Public Version Status
New
Public Device Record Key
c7650c59-2eea-4725-9121-b07c001b977b

Device Description

Disk ø 95 mm. H. 20 Pink

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EBF Material, Tooth Shade, Resin

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 08056099232152

Premarket Submissions

Submission Number Supplement Number
K173643 000

Device Sizes

Type Value Unit Text
Height 20 Millimeter